An expansion phase precedes terminal erythroid differentiation of hematopoietic progenitor cells from cord blood in vitro and is associated with up-regulation of cyclin E and cyclin-dependent kinase 2
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作者:
Dai, MS
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机构:Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
Dai, MS
Mantel, CR
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机构:Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
Mantel, CR
Xia, ZB
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机构:Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
Xia, ZB
Broxmeyer, HE
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机构:Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
Broxmeyer, HE
Lu, L
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机构:Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
Lu, L
机构:
[1] Indiana Univ, Sch Med, Walther Oncol Ctr, Indianapolis, IN 46202 USA
[2] Indiana Univ, Sch Med, Dept Microbiol Immunol, Indianapolis, IN 46202 USA
[3] Indiana Univ, Sch Med, Dept Med Hematol Oncol, Indianapolis, IN 46202 USA
The dynamics of cell cycle regulation were investigated during in vitro erythroid proliferation and differentiation of CD34(+) cord blood cells, An unusual cell cycle profile with a majority of cells in S phase (70.2%) and minority of cells in G1 phase (27.4%) was observed in burst-forming unit-erythrocytes (BFU-E)-derived erythroblasts from a 7-day culture of CD34(+) cells stimulated with interleukin 3 (IL-3), granulocyte-macrophage colony-stimulating factor (GM-CSF), Steel factor, and Epo. Terminal erythroid differentiation was accompanied by a rapid increase of G0/G1 phase cells. Expression of cyclin E and cyclin-dependent kinase 2 (cdk2) correlated with the proportion of S phase cells. Cyclin D3 was moderately up-regulated during the proliferation phase, and both cyclin E and D3 were rapidly down-regulated during terminal differentiation. This suggests that the high proliferation potential of erythroblasts is associated with temporal up-regulation of cyclin E and cdk2. (C) 2000 by The American Society of Hematology.